Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Chia‐Tse Weng"'
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-11 (2024)
Abstract Background Anti-Ro-52 antibodies have been associated with interstitial lung disease (ILD) in various autoimmune diseases. However, their role in ILD among patients with idiopathic inflammatory myopathies (IIMs) is relatively underexplored.
Externí odkaz:
https://doaj.org/article/2b80548ec4814d7988bce52699dade94
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
ObjectiveChildren of women with systemic lupus erythematosus (SLE) are at risk for childhood-onset SLE (cSLE). This study evaluated the incidence of early-onset cSLE and associated risk factors, including concomitant maternal and paternal autoimmune
Externí odkaz:
https://doaj.org/article/f12b3f7a2a0349c6bef9a1900106b810
Autor:
Hung-An Chen, Tsai-Ching Hsu, Su-Ching Yang, Chia-Tse Weng, Chun-Hsin Wu, Chien-Yao Sun, Chun-Yu Lin
Publikováno v:
Arthritis Research & Therapy, Vol 21, Iss 1, Pp 1-8 (2019)
Abstract Background No population-based study has investigated the cumulative incidence of pulmonary arterial hypertension (PAH) in patients with newly diagnosed systemic lupus erythematosus (SLE) or the survival impact of PAH in this population. Met
Externí odkaz:
https://doaj.org/article/9cc9972559fd496a9f92868386be152f
Publikováno v:
Respirology Case Reports, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Relapsing polychondritis (RP) is a rare autoimmune disorder, characterized by the inflammation of cartilaginous structures and proteoglycan‐rich tissues. Due to its rarity and the notoriously variable presentations, the diagnosis of RP cou
Externí odkaz:
https://doaj.org/article/8c28320f82ef4dc89b61a20b75aa383b
Publikováno v:
Healthcare, Vol 9, Iss 5, p 615 (2021)
Background: Pulmonary arterial hypertension (PAH) is a life-threatening disease with different etiologies and outcomes. We aimed to explore differences in clinical features and outcomes of idiopathic PAH (iPAH) and connective tissue disease-related P
Externí odkaz:
https://doaj.org/article/b3497b5cf33a454a876af66595969963
Autor:
Wen-Shuo Kuo, Chia-Tse Weng, Jian-Hua Chen, Chao-Liang Wu, Ai-Li Shiau, Jeng-Long Hsieh, Edmund Cheung So, Po-Ting Wu, Shih-Yao Chen
Publikováno v:
Nanomaterials, Vol 9, Iss 6, p 909 (2019)
Accumulated evidence suggests a pathogenic role of reactive oxygen species (ROS) in perpetually rheumatoid joints. Therefore, the application of radical scavengers for reducing the accumulation of ROS is beneficial for patients with rheumatoid arthri
Externí odkaz:
https://doaj.org/article/f73bdfee1174497e8c5844b0219416ce
Autor:
Hung-Ling Huang, Wen-Chih Lin, Wei-Lun Tsai, Chia-Tse Weng, Meng-Yu Weng, Chun-Hsin Wu, Yuan-Ting Sun
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 23; Pages: 6972
The mutual exclusivity of myositis-specific antibodies (MSAs) has been reported before, but the coexistence of 2 or more MSAs was still found in a few case reports. This study aims to confirm the existence and prevalence of double MSAs in patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8963c3ee8bd01863a1534ada3ad9c66
https://pubmed.ncbi.nlm.nih.gov/36498547
https://pubmed.ncbi.nlm.nih.gov/36498547
Publikováno v:
International Journal of Surgical Pathology. :106689692311573
Systemic lupus erythematosus (SLE) is an autoimmune disease with various clinical presentations. Mucin deposition is a characteristic finding in skin lesions, but it is rare in other organs. We present a case with erythematous patches from the termin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b652de1948b9f54a5c2a49e001761be
https://doi.org/10.1177/10668969231157313
https://doi.org/10.1177/10668969231157313
Autor:
Su Ching Yang, Chia Tse Weng, Chien Yao Sun, Chun Hsin Wu, Chun Yu Lin, Hung An Chen, Tsai-Ching Hsu
Publikováno v:
Arthritis Research & Therapy, Vol 21, Iss 1, Pp 1-8 (2019)
Arthritis Research & Therapy
Arthritis Research & Therapy
Background No population-based study has investigated the cumulative incidence of pulmonary arterial hypertension (PAH) in patients with newly diagnosed systemic lupus erythematosus (SLE) or the survival impact of PAH in this population. Method We us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6ed77db5c667a0c5bc09d06088fc714
http://link.springer.com/article/10.1186/s13075-019-1868-0
http://link.springer.com/article/10.1186/s13075-019-1868-0
Publikováno v:
Healthcare, Vol 9, Iss 615, p 615 (2021)
Healthcare
Volume 9
Issue 5
Healthcare
Volume 9
Issue 5
Background: Pulmonary arterial hypertension (PAH) is a life-threatening disease with different etiologies and outcomes. We aimed to explore differences in clinical features and outcomes of idiopathic PAH (iPAH) and connective tissue disease-related P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1179e82dffd80c3c12671fb9ec15d17f
https://www.mdpi.com/2227-9032/9/5/615
https://www.mdpi.com/2227-9032/9/5/615